Our focus is implementing clinical trials in physician's practices and increasing access to clinical research. We handle everything from study startup to closeout with no costs to the physician. We provide any research-specific equipment and manage every detail of the clinical trial process. Our goal is to empower physicians to offer better care to their patients with no risk and little burden. We provide the following services as part of site management: SOP development and implementation Study identification Execution of Confidentiality Disclosure Agreements Protocol feasibility Site selection process Contract and budget negotiation Regulatory and startup document completion IRB submission and correspondence Source document generation Site initiation Subject identification Subject study visits Study/site point of contact Study execution Monitoring visits and correspondence Drug/device accountability Electronic Data Capture entry Query resolution Study closeout Invoicing Marketing and advertising Record archiving